Health Condition 1: N944- Primary dysmenorrhea
Conditions
Interventions
None listed
Sponsors
Dr Denisha Chikhaliya
Eligibility
Inclusion criteria
Inclusion criteria: 1. Patients who are willing to participate in this study and gives informed written consent before trial. 2. Female in the age group of 18- 25 years. 3. Patients having regular menstrual cycle (21 to 35 days). 4. All the patients who are nulli or multipara women presenting with symptoms of Kashtaartava. 5. Patients who not take any kind of medication duration of trial.
Exclusion criteria
Exclusion criteria: 1.Female below the age of 18 years and above the 25 years age. 2.Patients having any pelvic pathology, Congenital anomalies, Acute infection, acyclic and excessive bleeding for more than 7 days, irregular menstrual cycle, Endometriosis, adenomyosis, uterine fibroid, endometrial polyp and other conditions resulting in dysmenorrhea. 3.Women suffering from systemic disease with organic lesion (benign or malignant growth of reproductive tract) any degree of prolapsed and hypoplastic uterus, polycystic ovarian disease (PCOD), any congenital abnormality of genital track.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Changes of VAS of pain during menstrual period. VAS score of 1-10 mm will be used for assessment.Timepoint: 1. Baseline - before starting the medicaments (first assessment) 2. After completion of 2 cycle of menstruation | — |
Secondary
| Measure | Time frame |
|---|---|
| Changes in symptoms & signs of dysmenorrhea. Present or absent of constipation, headache, nausea, fatigue, anorexia, vertigo & nervousness before & after the administration of medicaments.Timepoint: 1. Baseline - before starting the medicaments (first assessment) 2. After completion of 2 cycle of menstruation | — |
Countries
India
Contacts
Public ContactDr Denisha Chikhaliya
J.S. Ayurveda Mahavidyalaya
Outcome results
None listed